510(k) K850403 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
MEC DISTAL FEMORAL BOLT
| Applicant | Pfizer, Inc., Ny NY, US |
| Decision | Substantially Equivalent, Jul 15, 1985 |
| Received | Feb 1, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850403
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.